Abstract: There is provided a connector, for introducing or extracting a material to or from at least one receptacle, comprising a housing extending between a distal end and a proximal end, the housing comprising, at least at one end, a pierceable seal; a hollow needle mounted, at least partially, within the housing between the distal end and the proximal end of the housing, a first end of the hollow needle being connected or connectable to a first corresponding receptacle, and a second end of the hollow needle facing the pierceable seal at an end of the housing; and an actuating mechanism acting on the housing or the hollow needle to enable the hollow needle to pierce the pierceable seal thereby forming a communication through the pierceable seal, such that material is able to transfer through the connector.

Abstract: A suction catheter holder is provided. The holder can include a housing that defines an interior open-space compartment for receiving at least a portion of a suction catheter. The housing can have an elongate structure defined by a longitudinal and lateral axis. The housing can include a base panel having a substantially flat exterior surface, and a plurality of sidewalls, each extending upward from the base to a roof panel having an interior surface that faces, at least in part, an interior surface of the base panel. The housing can include a front sidewall panel extending laterally along the front edges of the base and roof panels, between a pair of longitudinal sidewalls. The front sidewall panel can include an insertion through-hole for receiving the suction catheter and a securing through-hole for retaining the suction catheter in place.

Abstract: A percutaneous drainage device for draining a fluid collection located under the skin of a patient is disclosed. The percutaneous drainage device includes a penetration component slidably engaged with a cannula. The penetration component has a piercing end adapted to penetrate tissue of a patient and introduce an open end of the cannula to a subcutaneous fluid collection site. The cannula may be held in place in the patient by an anchoring means. The cannula provides a passage through which a fluid collection may be drained from a patient. The cannula may be in fluid communication with a collection vessel, which collects fluid collection transported away from the subcutaneous fluid collection site.

Abstract: A wound irrigation system and method of making and using. The system uses a pored, closed-ended delivery conduit to enhance the consistency and speed with which anti-microbial or related irrigation fluids may be delivered in order to promote cleansing, debridement and biofilm reduction in wounds. The ease of use of the system as a moist wound healing cascade makes it applicable to both in-home and in-facility environments that is not offered through traditional instillation negative pressure systems. In one form, the fluid delivery conduit is used as part of a dual-conduit approach in order to also help promote the removal of drainage, waste, irrigation overflow or other fluid from the wound. Utilization of such a pored, closed-ended delivery conduit in conjunction with a separate drainage conduit infusing helps reduce the frequency of dressing changes as well as the likelihood of microorganism formation and colonization.

Abstract: An ocular implant for treating glaucoma is provided, which may include any number of features. More particularly, the present invention relates to implants that facilitate the transfer of fluid from within one area of the eye to another area of the eye. One feature of the implant is that it includes a proximal inlet portion and a distal inlet portion adapted to be inserted into the anterior chamber of the eye, and an intermediate portion adapted to be inserted into Schlemm's canal. Another feature of the implant is that it can be biased to assume a predetermined shape to aid in placement within the eye.

Abstract: A sanitary stoma system including at least eight absorbent sheets, with each of the sheets including absorbent plies. The plurality of absorbent sheets is arranged in a linear fashion and removably connected into a roll. The outermost absorbent sheet includes an adhesive such that the sanitary stoma system is configured into a stable roll useful for being placed upon a stoma of a user to absorb and contain bodily fluids excreted from the stoma, which may include urine or feces. Preferably, the sanitary stoma system is packaged in multiples of three and the sanitary stoma system is affixable to an abdomen of the user, configured to absorb bodily excretions.

Abstract: A pneumatic system for a medical fluid machine operating a medical fluid cassette, the pneumatic system including an interface for supplying positive pneumatic pressure and negative pneumatic pressure to the medical fluid cassette; a source of positive pneumatic pressure; a source of negative pneumatic pressure; and a pneumatic pump including a first head and a second head, wherein the first head is dedicated to supplying positive pneumatic pressure to the positive pneumatic pressure source and the second head is dedicated to supplying negative pneumatic pressure to the negative pneumatic pressure source.

Abstract: Minimally invasive catheter relates to the field of eversible catheters. It is primarily intended for use as a urinary catheter, but is also usable in other fields. As a urinary catheter this minimally invasive catheter 1 used as an indwelling or intermittent catheter with transurethral or suprapubic approach. This catheter has specific technical solution for eversible motion where tubular membrane 2, attached between distal part 36a of the handle 36 and distal part 3a of the inner tube 3, can in one case free slide between these two parts and in another be fixed to form hermetically sealed space 14. Free sliding of membrane ensures eversible principle of motion during placement and withdrawal of the catheter 1. Fixation of membrane allows a formation of hermetically sealed space 14 with fluid to make catheter surface smoother and softer, and a balloon 33 to hold catheter 1 in place for prolonged period of time.

Abstract: Ureteral or bladder catheters are provided, including (a) a proximal portion; and (b) a distal portion, the distal portion including a retention portion that includes one or more protected drainage holes, ports or perforations and is configured to establish an outer periphery or protective surface area that inhibits mucosal tissue from occluding the one or more protected drainage holes, ports or perforations upon application of negative pressure through the catheter. Systems, kits and methods for inducing negative pressure to increase renal function also are provided.

Abstract: A percutaneous drainage device for draining a fluid collection located under the skin of a patient is disclosed. The percutaneous drainage device includes a penetration component slidably engaged with a cannula. The penetration component has a piercing end adapted to penetrate tissue of a patient and introduce an open end of the cannula to a subcutaneous fluid collection site. The cannula may be held in place in the patient by an anchoring means. The cannula provides a passage through which a fluid collection may be drained from a patient. The cannula may be in fluid communication with a collection vessel, which collects fluid collection transported away from the subcutaneous fluid collection site.

Abstract: A method for removing excess fluid from a patient with hemodilution is provided. The method includes: deploying a urinary tract catheter into the patient such that flow of urine from the ureter and/or kidney is transported within a drainage lumen of the catheter; applying negative pressure to the ureter and/or kidney through the drainage lumen of the catheter to extract urine from the patient; periodically measuring a hematocrit value of the patient; and if the measured hematocrit value is greater than a predetermined threshold value, ceasing the application of the negative pressure to the ureter and/or kidney. A system for removing excess fluid from a patient with hemodilution including a ureteral catheter and a pump is also provided.

Abstract: An aortic perfusion catheter is an apparatus that is used during surgery for acute ascending aortic dissection to reduce postoperative injuries from profound hypothermia, ischemia, and reperfusion. The apparatus may include at least one main cannula, an inflation cannula, a drainage cannula, and a balloon tamponade. The at least one main cannula helps maintain blood perfusion to the body during the procedure to reduce postoperative injuries. The inflation cannula enables the selective inflation and deflation of the balloon tamponade to facilitate the insertion and removal of the balloon tamponade along with the at least one main cannula within the descending thoracic aorta. The balloon tamponade prevents blood flow into the operative area to maintain the operative area clear during the procedure. The drainage cannula enables the drainage of blood that may escape the balloon tamponade as well as other bodily fluids.

Abstract: System and method for bi-directional fluid injection includes a retrograde introducer, a retrograde cannula having an inlet opening, intermediate opening and outlet opening, an antegrade introducer and an antegrade cannula. The retrograde introducer is configured to engage with the retrograde cannula and to insert the retrograde cannula into a fluid channel. The antegrade introducer is configured to engage with the antegrade cannula and to insert the antegrade cannula into the fluid channel from within the retrograde cannula through the intermediate opening. After insertion of both cannulas, both introducers are removed. In operation, fluid flows into the retrograde cannula inlet and a portion thereof is diverted to the antegrade cannula which flows the portion in a first direction in the channel, the remainder of the fluid flows out the retrograde cannula outlet in an opposite direction in the channel. The system is removed from the channel using the introducers in reverse order.

Abstract: A trocar includes a shaft having a leading section, a trailing section, a reduced diameter midsection located between the leading and trailing sections, and a longitudinal axis extending along the length of the shaft. The leading section of the shaft has a tapered region that terminates at a blunt tip. The trailing section of the shaft has a connector located at the trailing end thereof. The leading and trailing sections of the shaft having a first diameter and the reduced diameter midsection of the shaft has a second diameter that is smaller than the first diameter for enabling the shaft to be bent at the reduced diameter midsection. A flexible wound drain catheter having a first end is secured to the connector at the trailing end of the trailing section of the shaft. The flexible wound drain catheter has an outer diameter that matches the first diameter of the leading and trailing sections of the shaft.

Abstract: A waste collection unit for collecting medical waste through a suction line. The waste collection unit includes a manifold receiver having an opening in fluid communication with a canister. A suction pump is configured to draw a vacuum, and a vacuum regulator is configured to regulate the vacuum draw. A light assembly positioned near the opening of the manifold receiver may include a first light and a second light. The light assembly may be arranged to direct the first light towards a manifold configured to be removably received in the manifold receiver. The light assembly may be arranged to direct the second light arcuately around at least a portion of the opening of the manifold receiver. The first light may emit light of different colors based on a commanded or measured level of the vacuum draw.

Abstract: A collection system for collecting outflow from a hysteroscopic surgical procedure includes a collection vessel and a mounting stand. The collection vessel defines an internal volume and includes a top portion and a bottom portion. The collection vessel is transitionable between a collapsed configuration and an expanded configuration. The mounting stand includes an upper retainer and a lower retainer. The upper retainer of the mounting stand is configured to retain the top portion of the collection vessel and the lower retainer of the mounting stand is configured to retain the bottom portion of the collection vessel. The upper and lower retainers are configured to retain the collection vessel thereon in the expanded configuration.

Abstract: A catheter comprising: a shaft (1) having a proximal end (2) and a distal end (3), the distal end terminating in a tip (4); a drainage opening (7) located at the distal end of the shaft, the drainage opening communicating with a drainage lumen (8) of the shaft; a balloon located at the distal end of the shaft, the balloon comprising a first region secured to the shaft, a second region secured to the shaft and an elastic-walled conduit extending between the first region and the second region, the elastic conduit extending over the tip.

Abstract: The present disclosure discloses a nephrostomy tube and a nephrostomy tube with curved drainage. The nephrostomy tube with curved drainage includes a bending head, a balloon element, and an elongated main body integrally connected with each other, wherein the nephrostomy tube with curved drainage has an guiding channel adapted for a guiding member to penetrate through, wherein the bending head has a first inner channel and at least two drainage bending channels located on the outer side of the first inner channel, wherein the balloon element has an air chamber and a second inner channel, wherein the at least two drainage bending channels are communicated with the second inner channel, wherein the elongated main body has a third inner channel communicated with the second inner channel of the balloon element, wherein the first inner channel, the second inner channel and the third inner channel from the guiding channel.

Abstract: This invention relates to a surgical smoke evacuation system for use in removing gases and smoke created in surgical procedures form within an insufflated surgical cavity, Such a system comprises a discharge assembly adapted to form a gases path, and having an end which in use is located within said surgical cavity so that gases and/or surgical smoke inside said cavity can pass out of said cavity and through said discharge assembly along said gases path, a flexible discharge limb having an operational site end and an outlet end, and a self-supporting wall defining a gases flow passage between said operational site end and said outlet end, in use said open operational site end sealingly connected to said discharge assembly so that said gases and/or surgical smoke can pass out of said discharge assembly and into said discharge limb, a filter connected in use to the outlet end of the discharge limb, at least part of said wall of the discharge limb formed from a breathable material, said breathable material allow

Abstract: An adapter for an evacuator for increasing a suction power of the evacuator includes a suction assembly adapted to be coupled with the evacuator. The suction assembly has a housing, an impeller arranged inside the housing and configured to provide a suction, and an inlet conduit to facilitate a flow of fluid to the impeller. The suction assembly also includes an outlet conduit arranged inside the housing and adapted to be coupled to the evacuator. The outlet conduit is in fluid communication with the impeller and facilitates a flow of the fluid from the suction assembly to the evacuator.